Pharmacological Reviews Get Tables of Contents delivered automatically
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     



0031-6997/07/5901-14-39$7.00
Pharmacol Rev 59:14-39, 2007

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yi, J. J.
Right arrow Articles by Ehlers, M. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Yi, J. J.
Right arrow Articles by Ehlers, M. D.

Emerging Roles for Ubiquitin and Protein Degradation in Neuronal Function

Jason J. Yi and Michael D. Ehlers

Program in Cell and Molecular Biology (J.J.Y., M.D.E.), Department of Pharmacology and Cancer Biology (J.J.Y., M.D.E.), Department of Neurobiology (M.D.E.), and Howard Hughes Medical Institute (M.D.E.), Duke University Medical Center, Durham, North Carolina

Abstract
I. Introduction
    A. Components of the Ubiquitin-Proteasome System
        1. Ubiquitin, E1, and E2.
        2. E3 Ubiquitin Ligases.
        3. The 26S Proteasome.
        4. Deubiquitinating Enzymes.
        5. Ubiquitin-Proteasome System Adaptor Proteins.
    B. Endoplasmic Reticulum-Associated Degradation
    C. Monoubiquitination and the Endocytic Pathway
II. The Ubiquitin-Proteasome System in Neuronal Function
    A. Neuronal Development
        1. Axon Growth, Steering, and Pruning.
        2. Synapse Formation and Elimination.
    B. Presynaptic Function
    C. Postsynaptic Plasticity
        1. The Ubiquitin-Proteasome System in Long-Term Potentiation.
        2. Ubiquitin-Proteasome System-Dependent Remodeling of the Postsynaptic Density.
    D. Ubiquitin and Postsynaptic Receptor Trafficking
        1. Glutamate Receptor Regulation in Caenorhabditis elegans.
        2. Glutamate Receptor Regulation in Mammals.
        3. Trafficking of GABA and Acetylcholine Receptors.
III. The Ubiquitin-Proteasome System in Neurological Disease
    A. Ubiquitin-Proteasome System-Linked Animal Models for Neurodegeneration
    B. Spinocerebellar Ataxia
    C. Parkinson's Disease
        1. Ubiquitin C-Terminal Hydrolase-L1 in Parkinson's Disease.
        2. Parkin.
    D. Neurodevelopmental Disorders: Angelman Syndrome
IV. Conclusions and Perspectives
Alterations in cellular structure and synapse composition are central to proper nervous system function. Recent work has identified the ubiquitin-proteasome system (UPS) as a key regulator of neuronal biology. The UPS is essential for the growth and development of immature neurons and is a criticalmediator of synaptic adaptability in mature neurons. Furthermore, proteinaceous deposits that accumulate in diverse neurodegenerative disorders are enriched in components of the UPS, suggesting that UPS dysfunction may be pivotal for pathogenesis. Here, we summarize existing knowledge about the role of the UPS in brain function, highlighting recent work delineating its importance in neuronal development, plasticity, and degeneration.


Address correspondence to: Dr. Michael D. Ehlers, HHMI, Department of Neurobiology, Duke University Medical Center, Box 3209, Durham, NC 27710. E-mail: ehlers{at}neuro.duke.edu




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
A. Varshavsky
Discovery of Cellular Regulation by Protein Degradation
J. Biol. Chem., December 12, 2008; 283(50): 34469 - 34489.
[Full Text] [PDF]


Home page
J. Neurosci.Home page
L. Bedford, D. Hay, A. Devoy, S. Paine, D. G. Powe, R. Seth, T. Gray, I. Topham, K. Fone, N. Rezvani, et al.
Depletion of 26S Proteasomes in Mouse Brain Neurons Causes Neurodegeneration and Lewy-Like Inclusions Resembling Human Pale Bodies
J. Neurosci., August 13, 2008; 28(33): 8189 - 8198.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Jurd, C. Thornton, J. Wang, K. Luong, K. Phamluong, V. Kharazia, S. L. Gibb, and D. Ron
Mind Bomb-2 Is an E3 Ligase That Ubiquitinates the N-Methyl-D-aspartate Receptor NR2B Subunit in a Phosphorylation-dependent Manner
J. Biol. Chem., January 4, 2008; 283(1): 301 - 310.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. Setoyama, M. Yamashita, and N. Sagata
Mechanism of degradation of CPEB during Xenopus oocyte maturation
PNAS, November 13, 2007; 104(46): 18001 - 18006.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. Rezvani, Y. Teng, D. Shim, and M. De Biasi
Nicotine Regulates Multiple Synaptic Proteins by Inhibiting Proteasomal Activity
J. Neurosci., September 26, 2007; 27(39): 10508 - 10519.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition
Copyright © 2007 by the American Society for Pharmacology and Experimental Therapeutics